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Idramantone → 5-Hydroxy-adamantan-2-one oxime

HRID 12816
Notes
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Reaction equation

HRID 12816 reaction equation
[OH:1][C:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([C:5]3=O)[CH2:3]1)[CH2:9]2.Cl.[NH2:14][OH:15]>CCO.[OH-].[Na+]>[OH:1][C:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([C:5]3=[N:14][OH:15])[CH2:3]1)[CH2:9]2
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 64184IdramantoneHCID 443297Hydroxyamine hydrochloride

Product 1

HCID 230089835-Hydroxy-adamantan-2-one oximeYield 73.4%

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 14798Sodium HydroxideSolvent

Conditions

Temperature
100 °C

Procedure

5-Hydroxy-2-admantanone (15 g, 90.2 mmol, CAS #: 20098-14-0, purchased from TCI) was dissolved in EtOH (100 mL) and added to a solution of hydroxylamine hydrochloride (10 g, 143.9 mmol) in 1N NaOH (80 mL). The mixture was heated at 100° C. for 2 hours. The EtOH was evaporated, and water and dichloromethane were added. The resulting mixture was stirred for 10 min and then filtered. The solid was collected. The resulting mixture was separated. The aqueous layer was further extracted twice with dichloromethane. The combined organic phases were concentrated under high vacuum. The resulting residue was combined with the solid from the filtration. Crystallization from EtOAc gave 5-hydroxy-adamantan-2-one oxime (12 g, 73%). Mass spectrum: m/z: 182 (M+1).

Workup

  1. customThe EtOH was evaporated
  2. additionwater and dichloromethane were added
  3. filtrationfiltered
  4. customThe solid was collected
  5. customThe resulting mixture was separated
  6. extractionThe aqueous layer was further extracted twice with dichloromethane
  7. concentrationThe combined organic phases were concentrated under high vacuum
  8. filtrationThe resulting residue was combined with the solid from the filtration
  9. customCrystallization from EtOAc

Sources & evidence

ORD record
ord-c831c44eb924457a978b16137d236615
Source dataset
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07728029B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes